Ckip-1 Regulates Mammalian and Zebrafish Myoblast Fusion
Year: 2012
Type: article
Abstract: Multinucleated muscle fibres arise by fusion of precursor cells called myoblasts. We previously showed that CKIP-1 ectopic expression in C2C12 myoblasts increased cell fusion. In this work, we report that CKIP-1 depletion drastically impairs C2C12 myoblast fusion in vitro and in vivo during zebrafish muscle development. Within developing fast-twich myotome, Ckip-1 localises at the periphery of fast precursor cells, closed to the plasma membrane. Unlike wild-type myoblasts that form spatially arrayed multinucleated fast myofibres, Ckip-1-deficient myoblasts show a drastic reduction in fusion capacity. A search for CKIP-1 binding partners identified the ARPC1 subunit of Arp2/3 actin nucleation complex essential for myoblast fusion. We demonstrate that CKIP-1, through binding to plasma membrane phosphoinositides via its PH domain, regulates cell morphology and lamellipodia formation by recruiting the Arp2/3 complex at the plasma membrane. These results establish CKIP-1 as a regulator of cortical actin that recruits the Arp2/3 complex at the plasma membrane essential for muscle precursor elongation and fusion.
Source: Journal of Cell Science
DOI: 10.1242/jcs.101048
Institutions: École Normale Supérieure de Lyon, Centre National de la Recherche Scientifique, Université de Lyon, Laboratoire de Biologie et Modélisation de la Cellule, Institut de Génomique Fonctionnelle de Lyon, Observatoire Océanologique de Banyuls-sur-Mer, Université Pierre-et-Marie-Curie, Harvard University, Dana-Farber Cancer Institute
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: green
Funder: Agence Nationale de la Recherche
OpenAlex ID: W2145911066
